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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall PKG, CLAW FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, CLAW FORCEPS, DOUBLE ACTION Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OPVIOPSY FORCEPS, SPOON JAW Stryker Endoscopy 2 United States USFDA
Device Recall PKG, OPERATING SCISSORS, SERRATED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MARYLAND FORCEPS, CURVED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MIXTER FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BABCOCK FORCEPS, PADDLE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, PKG, HOOK SCISSORS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, NEEDLE NOSE FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, PKG, PERITONEAL SCISSORS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, STRAIGHT, LONG Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, STRAIGHT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, METZENBAUM SCISSORS, CURVED LONG Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MINI METZENBAUM SCISSORS, CURVED LONG, Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ENDO METZENBAUM SCISSORS, CURVED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, ATRAUMATIC FORCEPS, DOUBLE ACTION Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MICRO SCISSORS, STRAIGHT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MICRO SCISSORS, CURVED Stryker Endoscopy 2 United States USFDA
Device Recall PKG, DOLPHIN FORCEPS, SERRATED SPOON Stryker Endoscopy 2 United States USFDA
Device Recall PKG, BULLET FORCEPS, TAPERED, SERRATED, SPOON Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MARYLAND FORCEPS, CURVED LEFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, KELLY FORCEPS, CURVED LEFT Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, TISSUE Stryker Endoscopy 2 United States USFDA
Device Recall PKG, MIXTER FORCEPS Stryker Endoscopy 2 United States USFDA
Device Recall PKG, GRASPER FORCEPS, SERRATED Stryker Endoscopy 2 United States USFDA